4.7 Article

A novel Apt-SERS platform for the determination of cardiac troponin I based on coral-like silver-modified magnetic substrate and BCA method

期刊

ANALYTICA CHIMICA ACTA
卷 1225, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.aca.2022.340253

关键词

Surface-enhanced Raman scattering; BCA method; Coral-like nano-sliver; Cardiac troponin I

资金

  1. National Natural Science Foundation of China [81860633]
  2. Natural Science Foundation of Guangxi [2019GXNSFDA245025]

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This study successfully constructed a high sensitivity Apt-SERS platform for protein quantification by preparing a magnetic nanoparticle substrate coated with coral-like nano-silver and combining aptamer modification. Combining BCA method and SERS detection technology, the platform achieved specific detection of cardiac troponin I (cTnI) and provided a new method for the detection and analysis of specific proteins.
As a kind of acute cardiovascular disease, acute myocardial infarction (AMI) endangers human's life and fitness seriously. The detection of cardiac troponin I (cTnI), a biomarker of AMI, is the key to early medical prognosis and treatment. Surface-enhanced Raman spectroscopy is viewed to be an effective approach for detection of low-concentration substances, and aptamers are regarded to be effective fragments to recognize proteins specifically. In this work, a magnetic nanoparticle substrate coated with coral-like nano-silver was prepared, and the aptamer-modified substrate Fe3O4@PEI/Ag NC-Apt was used as magnetic capture probe. Combined with BCA method and SERS detection technology, an Apt-SERS platform was successfully constructed and used for high sensitivity quantitative detection of protein. Taking cTnI as the target, the detection range of the proposed Apt-SERS platform was 0.001-100 ng mL(-1), and the estimated detection of limit (LOD) was 0.23 pg mL(-1). The recovery and relative standard deviations (RSD) of spiked experiment in human serum samples were 92-106% and 3.8-10.1%, respectively. The platform combining BCA method and SERS provides a high sensitivity and good reproducibility method for cTnI detection, which offers a new method for the specific detection and analysis of proteins.

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